Guiochon-Mantel A - Search Results

1

Upper limb onset of hereditary transthyretin amyloidosis is common in non-endemic areas.

Théaudin M, Lozeron P, Algalarrondo V, Lacroix C, Cauquil C, Labeyrie C, Slama MS, Adam C, Guiochon-Mantel A, Adams D; French FAP Network (CORNAMYL) Study Group. Théaudin M, et al. Among authors: guiochon mantel a. Eur J Neurol. 2019 Mar;26(3):497-e36. doi: 10.1111/ene.13845. Epub 2018 Dec 11. Eur J Neurol. 2019. PMID: 30350904

2

Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation).

Rousseau A, Terrada C, Touhami S, Barreau E, Rothschild PR, Valleix S, Benoudiba F, Errera MH, Cauquil C, Guiochon-Mantel A, Adams D, Labetoulle M. Rousseau A, et al. Am J Ophthalmol. 2018 Aug;192:169-177. doi: 10.1016/j.ajo.2018.05.023. Epub 2018 May 30. Am J Ophthalmol. 2018. PMID: 29859145

3

Conjunctival lymphangiectasia: a novel ocular manifestation of hereditary transthyretin amyloidosis.

Hayek S, Adam C, Adams D, Cauquil C, Barreau E, Guiochon-Mantel A, Labetoulle M, Rousseau A. Hayek S, et al. Among authors: guiochon mantel a. Amyloid. 2019 Jun;26(2):94-95. doi: 10.1080/13506129.2019.1594760. Epub 2019 May 10. Amyloid. 2019. PMID: 31074309 No abstract available.

4

Potential Role of In Vivo Confocal Microscopy for Imaging Corneal Nerves in Transthyretin Familial Amyloid Polyneuropathy.

Rousseau A, Cauquil C, Dupas B, Labbé A, Baudouin C, Barreau E, Théaudin M, Lacroix C, Guiochon-Mantel A, Benmalek A, Labetoulle M, Adams D. Rousseau A, et al. JAMA Ophthalmol. 2016 Sep 1;134(9):983-9. doi: 10.1001/jamaophthalmol.2016.1889. JAMA Ophthalmol. 2016. PMID: 27367055

5

The Roussy-Lévy family: from the original description to the gene.

Planté-Bordeneuve V, Guiochon-Mantel A, Lacroix C, Lapresle J, Said G. Planté-Bordeneuve V, et al. Ann Neurol. 1999 Nov;46(5):770-3. doi: 10.1002/1531-8249(199911)46:5<770::aid-ana13>3.0.co;2-u. Ann Neurol. 1999. PMID: 10553995

6

Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation.

Pingault V, Guiochon-Mantel A, Bondurand N, Faure C, Lacroix C, Lyonnet S, Goossens M, Landrieu P. Pingault V, et al. Ann Neurol. 2000 Oct;48(4):671-6. Ann Neurol. 2000. PMID: 11026454

7

Clinicopathological aspects of the neuropathy of neurogastrointestinal encephalomyopathy (MNGIE) in four patients including two with a Charcot-Marie-Tooth presentation.

Said G, Lacroix C, Planté-Bordeneuve V, Messing B, Slama A, Crenn P, Nivelon-Chevallier A, Bedenne L, Soichot P, Manceau E, Rigaud D, Guiochon-Mantel A, Matuchansky C. Said G, et al. J Neurol. 2005 Jun;252(6):655-62. doi: 10.1007/s00415-005-0712-4. Epub 2005 Mar 7. J Neurol. 2005. PMID: 15742109

8

Distinctive Patterns of Transthyretin Amyloid in Salivary Tissue: A Clinicopathologic Study of 92 Patients With Amyloid-containing Minor Salivary Gland Biopsies.

Jamet MP, Gnemmi V, Hachulla É, Dhaenens CM, Bouchindhomme B, Delattre C, Glowacki F, Hatron PY, Lacour A, Lamblin N, Launay D, Leleu X, Guiochon-Mantel A, Valleix S, Maurage CA, Copin MC, Buob D. Jamet MP, et al. Am J Surg Pathol. 2015 Aug;39(8):1035-44. doi: 10.1097/PAS.0000000000000430. Am J Surg Pathol. 2015. PMID: 25828388

9

The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases.

Planté-Bordeneuve V, Parman Y, Guiochon-Mantel A, Alj Y, Deymeer F, Serdaroglu P, Eraksoy M, Said G. Planté-Bordeneuve V, et al. J Neurol. 2001 Sep;248(9):795-803. doi: 10.1007/s004150170096. J Neurol. 2001. PMID: 11596785

10

High plasma estradiol interacts with diabetes on risk of dementia in older postmenopausal women.

Carcaillon L, Brailly-Tabard S, Ancelin ML, Rouaud O, Dartigues JF, Guiochon-Mantel A, Scarabin PY. Carcaillon L, et al. Neurology. 2014 Feb 11;82(6):504-11. doi: 10.1212/WNL.0000000000000107. Epub 2014 Jan 29. Neurology. 2014. PMID: 24477111

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